Severity
Moderate
FDA Drug recall · Reported April 3, 2013
Presence of Foreign Substance(s): There is a potential for foreign particulate matter in the API.
Physicians Total Care, Inc. recalled PHYSICIANS TOTAL CARE, TETRACYCLINE, 500 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUT… - a moderate-severity action.
PHYSICIANS TOTAL CARE, TETRACYCLINE, 500 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUT… was recalled by Physicians Total Care, Inc. in April 3, 2013. Reason: Presence of Foreign Substance(s): There is a potential for foreign particulate matter in the API.. Check the official notice for the remedy. Verify recall #D-222-2013 with the FDA Drug before acting.
The recall
Physicians Total Care, Inc. issued this moderate-severity FDA Drug recall-Presence of Foreign Substance(s): There is a potential for foreign particulate matter in the API..
Sourced from official FDA Drug enforcement records. Verify recall #D-222-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-222-2013) was formally reported on April 3, 2013, with the manufacturer initiating the action on February 20, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Physicians Total Care, Inc. is listed as the recalling firm, operating out of Tulsa, OK. Federal records list the affected scope as 3660 capsules.
The documented reason for this recall is: Presence of Foreign Substance(s): There is a potential for foreign particulate matter in the API. Distribution data in the federal record shows the product reached: FL, NC, TX, CO, VA, SC, GA, KS, LA, MO. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
3660 capsules
Related Recalls
6
0 from same agency
PHYSICIANS TOTAL CARE, TETRACYCLINE, 500 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUTICALS USA, SELLERSVILLE PA 18960 NDC 54868-0025-09
Presence of Foreign Substance(s): There is a potential for foreign particulate matter in the API.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-222-2013 |
| Date reported | April 3, 2013 |
| Date initiated | February 20, 2012 |
| Recalling firm | Physicians Total Care, Inc. |
| Firm location | Tulsa, OK |
| Affected scope | 3660 capsules |
| Distribution | FL, NC, TX, CO, VA, SC, GA, KS, LA, MO |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
Xishentang Dongguan Trading Co, Ltd., dba Pretty-Life, of China · 2026-07-02
Diamond Wipes International, Inc. of Chino, California · 2026-07-02
· 2026-07-02
· 2026-07-02
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California · 2026-07-02
Compare this recall with AMASKY Nursing Pillows Recalled Due to Risk of Serious Inju… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported April 3, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.